Results 221 to 230 of about 1,311,956 (360)

Ligation Bias in Illumina Next-Generation DNA Libraries: Implications for Sequencing Ancient Genomes

, 2013
Andaine Seguin‐Orlando, Mikkel Schubert, Joël Clary, Julia Stagegaard, Marı́a Teresa Alberdi, José Luís Prado, Alfredo Prieto, Eske Willerslev, Ludovic Orlando   +8 more
openalex   +2 more sources

Profiling the circulating miRNAs in mice exposed to gram-positive and gram-negative bacteria by Illumina small RNA deep sequencing [PDF]

, 2015
Cheng‐Shyuan Rau, Shao‐Chun Wu, Johnson Chia‐Shen Yang, Tsu‐Hsiang Lu, Yi-Chan Wu, Yi‐Chun Chen, Siou-Ling Tzeng, Chia‐Jung Wu, Ching‐Hua Hsieh   +8 more
openalex   +1 more source

Nanopore and Illumina Sequencing Reveal Different Viral Populations from Human Gut Samples

, 2023
Cook R, Telatin A, Hsieh S, Newberry F, Tariq MA, Baker DJ, Carding SR, Adriaenssens EM.   +7 more
europepmc   +1 more source

De novo transcriptome assembly using Illumina sequencing and development of EST-SSR markers in a monoecious herb Sagittaria trifolia Linn. [PDF]

PeerJ, 2022
Tang H, Saina JK, Long ZC, Chen J, Dai C.   +4 more
europepmc   +1 more source

Cryptic Splicing of GAP43 mRNA is a Novel Hallmark of TDP‐43‐Associated ALS and AD

Advanced Science, EarlyView.
TDP‐43 dysfunction disrupts RNA processing, inducing cryptic exon 4a1 inclusion in GAP43 and reducing its protein levels. This aberrant splicing impairs axonal regeneration and contributes to neurodegeneration in ALS and AD. RNA‐seq of patient brains reveals GAP43 downregulation and 4a1 upregulation, identifying cryptic exon 4a1 as a potential ...
Mingming Yang, Qi Wang, Dongkun Kang, Shijia Wang, Yanli Jiang, Jian‐Zhi Wang, Chen Ming, Rong Liu, Jianlan Gu, Xiaochuan Wang   +9 more
wiley   +1 more source

Exome Sequencing Reveals the Genetic Architecture of Non‐syndromic Orofacial Clefts and Identifies BOC as a Novel Causal Gene

Advanced Science, EarlyView.
Nonsyndromic orofacial clefts (NSOFCs) are the most common craniofacial defects. Exome sequencing of 214 sporadic cases sheds new light on its genetic architecture and identifies many candidate pathogenic variants. Furthermore, functional studies establish BOC as a novel causal gene and reveal an unusual two‐locus model of inheritance via the epistatic
Qing He, Min Yu, Yuhua Jiao, Yizhu Xu, Xuqin Liang, Wenbin Huang, Linping Xu, Yuxia Hou, Zhanping Ren, Beile Lyu, Zhenwei Qian, Pengpeng Liu, Jing Zhou, Huimei Huang, Chunyan Yin, Huaxiang Zhao, Yi Ding   +16 more
wiley   +1 more source

Characterization of microsatellite loci for an Australian epiphytic orchid, Dendrobium calamiforme, using Illumina sequencing [PDF]

, 2015
Dorset W. Trapnell, Rochelle R. Beasley, Stacey L. Lance, Ashley R. Field, Kenneth L. Jones   +4 more
openalex   +1 more source

Integrative Analysis of Nanopore and Illumina Sequencing Reveals Alternative Splicing Complexity in Pig Longissimus Dorsi Muscle. [PDF]

Front Genet, 2022
Shu Z, Wang L, Wang J, Zhang L, Hou X, Yan H, Wang L.   +6 more
europepmc   +1 more source

IncRNA‐ZFAS1, an Emerging Gate‐Keeper in DNA Damage‐Dependent Transcriptional Regulation

Advanced Science, EarlyView.
LncZFAS1 plays a crucial role during DNA damage response in mammalian cells. Loss of lncZFAS1 results in deficient DNA lesion removal and reduced cell viability. Mechanistically, lncZFAS1 modulates RNAPII phosphorylation and transcription and thereby promotes both GG‐NER and TC‐NER upon UV damage.
Jiena Liu, Qing Lu, Zixuan Fan, Jiahui Lin, Nan He, Xin Zhang, Zhaoya Han, Tingting Zhu, Zhenzhen Wu, Yingying Xu, Yuming Wang   +10 more
wiley   +1 more source

94. AAV Integration Site Determination Using Illumina Mate Pair Sequencing [PDF]

, 2015
Matthew Tiffany, Mark A. Kay
openalex   +1 more source